The Rare Fair is a two-day global event designed to connect rare patients, caregivers, and advocates with the resources they need to manage a rare disease diagnosis.

At The Rare Fair, patients and caregivers can network directly with physicians, medical providers, non-profit organizations, and other rare stakeholders. Our goal is to bring together the best rare resources available so attendees can add those resources to their own diagnosis management network. 

If you do miss something during The Rare Fair, all content is available for 30 days after the event!